Canonical Allele Identifier: CA359721090
Gene: CCNO HGNC NCBI

Linked Data

ClinVar Variation Id: 1304537
ClinVar RCV Id: RCV001752304
dbSNP Id: rs2111714327
MyVariant Identifiers: chr5:g.54527449A>T (hg19) chr5:g.55231621A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.55231621A>T , CM000667.2:g.55231621A>T GRCh38
NC_000005.9:g.54527449A>T , CM000667.1:g.54527449A>T GRCh37
NC_000005.8:g.54563206A>T NCBI36
NG_034201.1:g.7097T>A
NG_051620.1:g.695T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282572.5:c.807T>A MANE Select ENSP00000282572.4:p.Ser269Arg
ENST00000282572.4:c.807T>A ENSP00000282572.4:p.Ser269Arg
ENST00000501463.2:c.*787T>A ENSP00000422485.1:n.*787T>A
NM_021147.4:c.807T>A NP_066970.3:p.Ser269Arg
NR_125346.1:n.1377T>A
NR_125347.1:n.1006T>A
NR_125348.1:n.871T>A
NM_021147.5:c.807T>A MANE Select NP_066970.3:p.Ser269Arg
NR_125346.2:n.1268T>A
NR_125347.2:n.897T>A
Search 100 bp 5'
Search 100 bp 3'